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基于扩增片段长度多态性(AFLP)技术将大麦Mlo基因精细定位到大麦基因组的一个30千碱基对(kb)的DNA区段。

AFLP-based fine mapping of the Mlo gene to a 30-kb DNA segment of the barley genome.

作者信息

Simons G, van der Lee T, Diergaarde P, van Daelen R, Groenendijk J, Frijters A, Büschges R, Hollricher K, Töpsch S, Schulze-Lefert P, Salamini F, Zabeau M, Vos P

机构信息

Keygene N.V., Wageningen, The Netherlands.

出版信息

Genomics. 1997 Aug 15;44(1):61-70. doi: 10.1006/geno.1997.4844.

Abstract

Resistance of barley (Hordeum vulgare) to the powdery mildew fungus Erysiphe graminis f.sp. hordei is conferred by several dominant genes, but also by recessive alleles of the Mlo locus mapping on the long arm of chromosome 4. In addition, this single-factor-mediated resistance is active against all known physiological races of the parasite. Thus the mechanism underlying mlo-mediated resistance should differ substantially from that mediated by the dominant genes. A positional cloning strategy to isolate the Mlo gene from the barley genome, the size of which is almost double the size of the human genome, has been designed. The AFLP technique was employed to identify markers tightly linked to the Mlo locus and to produce a local high-resolution genetic map. The use of this high-volume marker technology allowed the rapid screening of approximately 250,000 loci for linkage to Mlo. A large number of Mlo-linked AFLP markers were identified, one of which cosegregated with Mlo on the basis of more than 4000 meiotic events. A four-genome-equivalent barley YAC library (average insert size 480 kb) was constructed and screened with this cosegregating marker. Four YACs containing this marker were isolated and subsequent characterization by AFLP-based physical mapping allowed the physical delimitation of the Mlo locus to a DNA segment of 30 kb.

摘要

大麦(Hordeum vulgare)对禾本科布氏白粉菌(Erysiphe graminis f.sp. hordei)的抗性由多个显性基因决定,但也由位于4号染色体长臂上的Mlo位点的隐性等位基因决定。此外,这种单因子介导的抗性对该寄生菌的所有已知生理小种均有效。因此,mlo介导的抗性机制应与显性基因介导的抗性机制有很大不同。已设计出一种从大麦基因组中分离Mlo基因的定位克隆策略,大麦基因组的大小几乎是人类基因组大小的两倍。采用AFLP技术来鉴定与Mlo位点紧密连锁的标记,并构建局部高分辨率遗传图谱。使用这种大容量标记技术能够快速筛选约250,000个位点以寻找与Mlo的连锁关系。鉴定出大量与Mlo连锁的AFLP标记,其中一个基于4000多个减数分裂事件与Mlo共分离。构建了一个相当于四个基因组的大麦YAC文库(平均插入片段大小为480 kb),并用这个共分离标记进行筛选。分离出四个含有该标记的YAC,随后通过基于AFLP的物理图谱分析对其进行表征,从而将Mlo位点物理定位到一个30 kb的DNA片段上。

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